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resource source identifier pvsv g clontech  (TaKaRa)


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    Structured Review

    TaKaRa resource source identifier pvsv g clontech
    Resource Source Identifier Pvsv G Clontech, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 372 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pvsv+g/Retro-X+Universal+Packaging+System/pm41824454-675-2-6
    Average 96 stars, based on 372 article reviews
    resource source identifier pvsv g clontech - by Bioz Stars, 2026-09
    96/100 stars

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    Plasmid Preparation:

    Article Title: Engineering stable and non-immunogenic immunoenzymes for cancer therapy via in situ generated prodrugs.
    Article Snippet: Engineering human enzymes for therapeutic applications is attractive but introducing new amino acids may adversely affect enzyme stability and immunogenicity.. Here we used a mammalian membrane-tethered screening system (ECSTASY) to evolve human lysosomal beta-glucuronidase (hBG) to hydrolyze a glucuronide metabolite (SN-38G) of the anticancer drug irinotecan (CPT-11).. Three human beta-glucuronidase variants (hBG3, hBG10 and hBG19) with 3, 10 and 19 amino acid substitutions were identified that display up to 40-fold enhanced enzymatic activity, higher stability than E. coli beta-glucuronidase in human serum, and similar pharmacokinetics in mice as wild-type hBG.

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Transfection:

    Article Title: Engineering stable and non-immunogenic immunoenzymes for cancer therapy via in situ generated prodrugs.
    Article Snippet: Engineering human enzymes for therapeutic applications is attractive but introducing new amino acids may adversely affect enzyme stability and immunogenicity.. Here we used a mammalian membrane-tethered screening system (ECSTASY) to evolve human lysosomal beta-glucuronidase (hBG) to hydrolyze a glucuronide metabolite (SN-38G) of the anticancer drug irinotecan (CPT-11).. Three human beta-glucuronidase variants (hBG3, hBG10 and hBG19) with 3, 10 and 19 amino acid substitutions were identified that display up to 40-fold enhanced enzymatic activity, higher stability than E. coli beta-glucuronidase in human serum, and similar pharmacokinetics in mice as wild-type hBG.

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Article Title: Long Terminal Repeats of Gammaretroviruses Retain Stable Expression After Integration Retargeting or Knock-In into the Restrictive Chromatin of Lamina-Associated Domains
    Article Snippet: .. The next day, cells were co-transfected by the viral genome, Gag-Pol ( ; ; ), and pVSV-G (Clontech) constructs in 6:3:1 weight ratios by X-Treme Gene HP Transfection Reagent (Roche) or the calcium phosphate method. ..

    Article Title: Pauperization of Emerin from nuclear envelope during chromatin bridge resolution drives prostate cancer cell migration and invasiveness
    Article Snippet: EMD1 and EMD2 gRNA sequences were inserted via BsmBI restriction enzyme into plentiCRISPRv2_puro vector (Addgene, 52961) and applied for lentivirus preparation. .. Lentiviral particles were generated by co-transfecting 5 μg of the specific plentiCRISPRv2, 3.75 μg psPax2, and 1.25 μg pVSV-G (second-generation lentivirus packaging system) into human embryonic 10 kidney packaging cells GP2-293 (Clontech, Inc., Mountain View, CA, USA), using CalPhosTM Mammalian Transfection Kit (Clontech, Inc., Mountain View, CA, USA), according to the manufacturer’s protocol as described (58). ..

    Recombinant:

    Article Title: Engineering stable and non-immunogenic immunoenzymes for cancer therapy via in situ generated prodrugs.
    Article Snippet: Engineering human enzymes for therapeutic applications is attractive but introducing new amino acids may adversely affect enzyme stability and immunogenicity.. Here we used a mammalian membrane-tethered screening system (ECSTASY) to evolve human lysosomal beta-glucuronidase (hBG) to hydrolyze a glucuronide metabolite (SN-38G) of the anticancer drug irinotecan (CPT-11).. Three human beta-glucuronidase variants (hBG3, hBG10 and hBG19) with 3, 10 and 19 amino acid substitutions were identified that display up to 40-fold enhanced enzymatic activity, higher stability than E. coli beta-glucuronidase in human serum, and similar pharmacokinetics in mice as wild-type hBG.

    Retroviral:

    Article Title: Engineering stable and non-immunogenic immunoenzymes for cancer therapy via in situ generated prodrugs.
    Article Snippet: Engineering human enzymes for therapeutic applications is attractive but introducing new amino acids may adversely affect enzyme stability and immunogenicity.. Here we used a mammalian membrane-tethered screening system (ECSTASY) to evolve human lysosomal beta-glucuronidase (hBG) to hydrolyze a glucuronide metabolite (SN-38G) of the anticancer drug irinotecan (CPT-11).. Three human beta-glucuronidase variants (hBG3, hBG10 and hBG19) with 3, 10 and 19 amino acid substitutions were identified that display up to 40-fold enhanced enzymatic activity, higher stability than E. coli beta-glucuronidase in human serum, and similar pharmacokinetics in mice as wild-type hBG.

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Cell Culture:

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Virus:

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Expressing:

    Article Title: Targeting endogenous fatty acid synthesis stimulates the migration of ovarian cancer cells to adipocytes and promotes the transport of fatty acids from adipocytes to cancer cells
    Article Snippet: .. Briefly, 2×10 6 293T cells (Takara Bio USA, Inc.) maintained in DMEM plus 10% FCS were transfected in T25 cell culture flasks (Thermo Fisher Scientific, Inc.) by calcium phosphate co-precipitation with 5 μ g of the Moloney murine leukemia virus (MMLV)-derived retroviral expression plasmid pQCXIP (Takara Bio USA, Inc.) containing sequences for puromycin resistance and mCherry, and with 3.75 μ g p-gag-pol-gpt ( ) and 1.25 μ g pVSV-G (Takara Bio USA, Inc.) as helper plasmids. ..

    Article Title: A model of human neural networks reveals NPTX2 pathology in ALS and FTLD.
    Article Snippet: .. To generate mTRE-GFP-FUS, GFP-FUS sequence from Hock et al. 27 was substituted into mTRE-TDP-43–HA via HiFi Kit. mTRE-TDP-43–HA and all other lentiviruses were then packaged into lentivirus via Lipofectamine 2000 (Invitrogen 11668019; 8.3 μl per ml final volume) co-transfection with CMV-Gag-Pol (Harvard dR8.91) and pVSV-G (Clontech, part of 631530) plasmids into production HEK293T cells (ATCC CRL-3216; gift from the Greber laboratory) adapted to grow in serum-free conditions (OHN medium; based on Opti-MEM (ThermoFisher 11058-021), supplemented with 0.5% B27- (ThermoFisher 12587-010), 0.5% N2 (ThermoFisher 175020-01), 1% GlutaMAX (ThermoFisher 35050038) and bFGF (25 ng ml−1; ThermoFisher PHG0261)), which reduces the expression of the gene of interest from the transfer vector (that is, it eliminates traces of tetracyclines in the FBS) as well as eliminates serum-carry over into the lentivirus supernatant. .. Medium was changed the following morning and supernatants were then collected 48 h post transfection (36 h post-medium change), centrifuged (500g, 10 min, 4 °C), filtered through Whatman 0.45-μm CA filter (GE 10462100) and concentrated using Lenti-X Concentrator (Takara 631232) according to the producer instructions (overnight incubation).

    Article Title: A model of human neural networks reveals NPTX2 pathology in ALS and FTLD
    Article Snippet: .. To generate mTRE-GFP-FUS, GFP-FUS sequence from Hock et al. was substituted into mTRE-TDP-43–HA via HiFi Kit. mTRE-TDP-43–HA and all other lentiviruses were then packaged into lentivirus via Lipofectamine 2000 (Invitrogen 11668019; 8.3 μl per ml final volume) co-transfection with CMV-Gag-Pol (Harvard dR8.91) and pVSV-G (Clontech, part of 631530) plasmids into production HEK293T cells (ATCC CRL-3216; gift from the Greber laboratory) adapted to grow in serum-free conditions (OHN medium; based on Opti-MEM (ThermoFisher 11058-021), supplemented with 0.5% B27- (ThermoFisher 12587-010), 0.5% N2 (ThermoFisher 175020-01), 1% GlutaMAX (ThermoFisher 35050038) and bFGF (25 ng ml −1 ; ThermoFisher PHG0261)), which reduces the expression of the gene of interest from the transfer vector (that is, it eliminates traces of tetracyclines in the FBS) as well as eliminates serum-carry over into the lentivirus supernatant. .. Medium was changed the following morning and supernatants were then collected 48 h post transfection (36 h post-medium change), centrifuged (500 g , 10 min, 4 °C), filtered through Whatman 0.45-μm CA filter (GE 10462100) and concentrated using Lenti-X Concentrator (Takara 631232) according to the producer instructions (overnight incubation).

    Sequencing:

    Article Title: A model of human neural networks reveals NPTX2 pathology in ALS and FTLD.
    Article Snippet: .. To generate mTRE-GFP-FUS, GFP-FUS sequence from Hock et al. 27 was substituted into mTRE-TDP-43–HA via HiFi Kit. mTRE-TDP-43–HA and all other lentiviruses were then packaged into lentivirus via Lipofectamine 2000 (Invitrogen 11668019; 8.3 μl per ml final volume) co-transfection with CMV-Gag-Pol (Harvard dR8.91) and pVSV-G (Clontech, part of 631530) plasmids into production HEK293T cells (ATCC CRL-3216; gift from the Greber laboratory) adapted to grow in serum-free conditions (OHN medium; based on Opti-MEM (ThermoFisher 11058-021), supplemented with 0.5% B27- (ThermoFisher 12587-010), 0.5% N2 (ThermoFisher 175020-01), 1% GlutaMAX (ThermoFisher 35050038) and bFGF (25 ng ml−1; ThermoFisher PHG0261)), which reduces the expression of the gene of interest from the transfer vector (that is, it eliminates traces of tetracyclines in the FBS) as well as eliminates serum-carry over into the lentivirus supernatant. .. Medium was changed the following morning and supernatants were then collected 48 h post transfection (36 h post-medium change), centrifuged (500g, 10 min, 4 °C), filtered through Whatman 0.45-μm CA filter (GE 10462100) and concentrated using Lenti-X Concentrator (Takara 631232) according to the producer instructions (overnight incubation).

    Article Title: A model of human neural networks reveals NPTX2 pathology in ALS and FTLD
    Article Snippet: .. To generate mTRE-GFP-FUS, GFP-FUS sequence from Hock et al. was substituted into mTRE-TDP-43–HA via HiFi Kit. mTRE-TDP-43–HA and all other lentiviruses were then packaged into lentivirus via Lipofectamine 2000 (Invitrogen 11668019; 8.3 μl per ml final volume) co-transfection with CMV-Gag-Pol (Harvard dR8.91) and pVSV-G (Clontech, part of 631530) plasmids into production HEK293T cells (ATCC CRL-3216; gift from the Greber laboratory) adapted to grow in serum-free conditions (OHN medium; based on Opti-MEM (ThermoFisher 11058-021), supplemented with 0.5% B27- (ThermoFisher 12587-010), 0.5% N2 (ThermoFisher 175020-01), 1% GlutaMAX (ThermoFisher 35050038) and bFGF (25 ng ml −1 ; ThermoFisher PHG0261)), which reduces the expression of the gene of interest from the transfer vector (that is, it eliminates traces of tetracyclines in the FBS) as well as eliminates serum-carry over into the lentivirus supernatant. .. Medium was changed the following morning and supernatants were then collected 48 h post transfection (36 h post-medium change), centrifuged (500 g , 10 min, 4 °C), filtered through Whatman 0.45-μm CA filter (GE 10462100) and concentrated using Lenti-X Concentrator (Takara 631232) according to the producer instructions (overnight incubation).

    Construct:

    Article Title: Long Terminal Repeats of Gammaretroviruses Retain Stable Expression After Integration Retargeting or Knock-In into the Restrictive Chromatin of Lamina-Associated Domains
    Article Snippet: .. The next day, cells were co-transfected by the viral genome, Gag-Pol ( ; ; ), and pVSV-G (Clontech) constructs in 6:3:1 weight ratios by X-Treme Gene HP Transfection Reagent (Roche) or the calcium phosphate method. ..

    Generated:

    Article Title: Pauperization of Emerin from nuclear envelope during chromatin bridge resolution drives prostate cancer cell migration and invasiveness
    Article Snippet: EMD1 and EMD2 gRNA sequences were inserted via BsmBI restriction enzyme into plentiCRISPRv2_puro vector (Addgene, 52961) and applied for lentivirus preparation. .. Lentiviral particles were generated by co-transfecting 5 μg of the specific plentiCRISPRv2, 3.75 μg psPax2, and 1.25 μg pVSV-G (second-generation lentivirus packaging system) into human embryonic 10 kidney packaging cells GP2-293 (Clontech, Inc., Mountain View, CA, USA), using CalPhosTM Mammalian Transfection Kit (Clontech, Inc., Mountain View, CA, USA), according to the manufacturer’s protocol as described (58). ..



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